A new species of gecarcinucid freshwater crab of the genus Parathelphusa H. Milne Edwards, 1853, is described from freshwater swamp habitats in Pekanbaru, Riau Province, in central-eastern Sumatra, Indonesia. Parathelphusa pardus sp. nov., has a very distinctive colour pattern, and in this respect, resembles P. maindroni (Rathbun, 1902) from Sumatra and Peninsular Malaysia; P. batamensis Ng, 1992, from Batam Island, Indonesia; P. reticulata Ng, 1990, from Singapore; and P. oxygona Nobili, 1901, from western Sarawak. It can be distinguished from these species and congeners by a suite of carapace, ambulatory leg, thoracic sternal and most importantly, male first gonopod characters.
Horaeomorphus bicornis sp. n., a remarkable species with strongly modified head from Yunnan, Southwest China is described. A distinctly different female from the same locality is also recorded, its identity remains unconfirmed until associated males become available. The previously unknown female of H. hujiayaoi Zhou & Zhang, 2016, is discovered, with its spermatheca and female terminalia illustrated. Horaeomorphus punctatissimus Franz, 1992 is newly recorded from Mount Trus Madi, Malaysia. Two females of H. eumicroides Schaufuss, 1889 were discovered from Singapore, with female terminalia illustrated.
The areolate Oriental family Heteropterygidae Kirby, 1893 is critically reviewed and the results of the present study contradict the arrangement suggested by Zompro (2004), but in most aspects agree with a molecular study presented by Whiting et al (2003) and a phylogenetic study presented by Bradler (2009). The family is critically discussed and new hypotheses are presented for the phylogeny and intra-familiar relationships, placing the subfamily Dataminae Rehn & Rehn, 1939 as the basalmost clade of Heteropterygidae. The subfamilies Obriminae Brunner v. Wattenwyl, 1893 and Heteropteryginae Kirby, 1893 together represent the sister-group of Dataminae. Arguments and a tree are presented to support this hypothesis. New diagnoses and lists of genera are provided for all three subfamilies contained in Heteropterygidae, along with keys to distinguish between them. The subfamily Obriminae is critically reviewed and the distinction between the three tribes Obrimini Brunner v. Wattenwyl, 1893, Eubulidini Zompro, 2004 and Miroceramiini Zompro, 2004 introduced by Zompro (2004) is shown to be poorly supported. While Obrimini sensu Zompro, 2004 is generally accepted (but now also contains genera that were placed in Eubulidini or Miroceramiini by Zompro (2004)), the tribes Eubulidini and Miroceramiini are not supported. A new arrangement is introduced, which is based on morphological characters neglected or overlooked by Zompro (2004) but were partly discussed by Bradler (2009). The genus Mearnsiana Rehn & Rehn, 1939 is removed from Miroceramiini and transferred to Obrimini. The genera Eubulides Stål, 1877, Heterocopus Redtenbacher, 1906, Theramenes Stål, 1875 and Stenobrimus Redtenbacher, 1906 are removed from Eubulidini and also transferred to Obrimini. Consequently, Eubulidini is synonymised with Obrimini (n. syn.). Miroceramiini is a monotypical tribe and only includes the Wallacean genus Miroceramia Günther, 1934. The new tribe Tisamenini n. trib. is established for the three basal genera Tisamenus Stål, 1875, Ilocano Rehn & Rehn, 1939 and Hoploclonia Stål, 1875 all of which were placed in Eubulidini by Zompro (2004). The latter genus differs from the other two genera by the morphology of the female genitalia, which is unique amongst the entire family. Three generic groups are recognized within Obrimini, the Obrimus-group, Stenobrimus-group and Theramenes-group. Keys are presented to distinguish between the three tribes now contained in the Obriminae, i.e. Obrimini, Tisamenini n. trib. and Miroceramiini. The genus Hennobrimus Conle, 2006 is synonymised with Mearnsiana Rehn & Rehn, 1939, based on the fact that the type-species of both genera are conspecific (n. syn.). Hennobrimus hennemanni Conle, 2006, the type-species of Hennobrimus, and Trachyaretaon manobo Lit & Eusebio, 2005 are synonymised with Mearnsiana bullosa Rehn & Rehn, 1939, the type-species of Mearnsiana (n. syn.). Theramenes dromedarius Stål, 1877 from the Philippines is removed from synonymy with the Wallacean Theramenes olivaceus (Westwood, 1859) and re-established as a valid species (rev. stat.). The subfamily Heteropteryginae Kirby, 1896 is revised at the species-level and a new diagnosis is presented. Keys to the two genera and all 16 known species are provided along with new descriptions, differential diagnoses, lists of examined material, detailed information on the known distributions, measurements and illustrations of the insects and eggs. The intra-subfamiliar and intra-generic relationships are discussed and a cladogram is presented. Heteropteryginae contains two genera: Heteropteryx Gray, 1835 (Type-species: Phasma dilatatum Parkinson, 1798) and Haaniella Kirby, 1896 (Type-species: Phasma (Heteropteryx) muelleri de Haan, 1842). The distribution of this subfamily is restricted to Sundaland with the exception of a single species that is found in Vietnam. All other species are distributed in Borneo, Sumatra, the Mentawai Islands, Singapore, Peninsular Malaysia and Thailand. Heteropteryginae contains the largest and most striking members of the entire family Heteropteryginae, some of which are amongst the heaviest insects known. The subfamily is characterized by apomorphies such as the presence of wings, having a tympanal area (= stridulatory organ) in the basal portion of the alae, straight profemora, strongly shortened tarsi, lack of rough sensory-areas on the prosternum and typically X-shaped micropylar plate of the eggs. The sister-group of Heteropteryginae is represented by the Obriminae, with which it shares a beak-like secondary ovipositor in the females and presence of a medio-apical spine on the area apicalis. Both features are synapomorphies of Heteropteryginae + Obriminae. The genus Haaniella Kirby, 1904 contains 16 known species, five of which are newly described herein. The genus Miniopteryx Zompro, 2004 (Type-species: Haaniella parva Günther, 1944) is synonymised with Haaniella on the basis that the distinguishing feature mentioned in the original description is a character that is frequently found throughout the genus (n. syn.). The type-species H. parva Günther, 1944 is automatically retransferred to Haaniella (rev. stat.). Haaniella aculeata n. sp. from western Sumatra is described from the male. Haaniella macroptera n. sp. from Singapore and the Johor state in southern Peninsular Malaysia is described from both sexes and the eggs. Haaniella gintingi n. sp. from Central Sumatra is described from both sexes and the eggs and Haaniella kerincia n. sp. from Western Sumatra is described from the insects only, the eggs being still unknown. One new species, Haaniella gorochovi n. sp., is the only representative of the genus and subfamily Heteropteryginae known from Vietnam and both sexes as well as the eggs are described. Haaniella erringtoniae (Redtenbacher, 1906) is endemic in Peninsular Malaysia, here removed from synonymy with H. muelleri (de Haan, 1842) and re-established as a valid species (rev. stat.). The Sumatran Haaniella glaber (Redtenbacher, 1906) is removed from synonymy with H. muelleri (Haan, 1842) and re-established as a valid species (rev. stat.). Leocrates glaber Redtenbacher, 1906 and Haaniella muelleri simplex Günther, 1944 are removed from synonymy with H. muelleri (Haan, 1842) (rev. stat.) and synonymised with H. glaber. Haaniella mecheli (Redtenbacher, 1906) and H. rosenbergii (Kaup, 1871) are removed from synonymy with H. muelleri (Haan, 1842) and re-established as valid species (rev. stat.). Haaniella erringtoniae novaeguineae Günther, 1934 and Haaniella muelleri var. b. (Haan, 1842) are synonymized with H. rosenbergii (Kaup, 1871) (n. syn.). The type-species Haaniella muelleri (Haan, 1842) is shown to be a fairly rare species that is restricted to Sumatra. All subsequent records of H. muelleri from outside Sumatra and references to captive breeding of stock originating from Peninsular Malaysia in Europe relate to H. erringtoniae (Redtenbacher, 1906). The previously unknown males and eggs of H. rosenbergii (Kaup, 1871) as well as the previously unknown females and eggs of H. parva Günther, 1944 are described and illustrated for the first time. Based on morphological characters of the insects and eggs three distinct species-groups are recognized within Haaniella. The muelleri species-group contains nine species that are distributed throughout Sumatra, the Mentawei Islands, Singapore and Peninsular Malaysia. These are characterized by the smooth ventral surface of the meso- and metafemora and lemon-shaped eggs which entirely lack the setae seen in the two other species-groups. The grayii species-group comprises four species, two of which are endemic in Borneo, one endemic in Sumatra and the fourth species being the only known representative of the subfamily in Vietnam. These species are characteristic for the prominent pair of spines on the abdominal tergites II-IV of males and long apically multidentate epiproct of females. The echinata species-group contains three exceptionally Bornean species, which are characterized by the long and apically pointed subgenital plate of females, which clearly projects beyond the epiproct, as well as the sub-basal lateral tooth of the anal segment of males. The muelleri species-group is sister to the remainder two species-groups. Heteropteryx Gray, 1853 is a monotypical genus and only contains the type-species H. dilatata (Parkinson, 1798), which is found throughout Peninsular Malaysia, Thailand, Sumatra and Northeastern Borneo. This genus differs from Haaniella by the strongly conically elevated head, which posteriorly projects over the anterior margin of the pronotum, females being bright green or yellow in colour with plain and translucent pink alae and having distinct spines on the abdominal tergites, and males having a strongly shortened mesothorax and dull pink alae. Lectotypes are designated for Haaniella parva Günther, 1944, Heteropteryx echinata Redtenbacher, 1906, Heteropteryx saussurei Redtenbacher, 1906 and Heteropteryx scabra Redtenbacher, 1906 to guarantee stability of these names. Information on the habitats, host-plants, biology, life cycle, parasitism and captive breeding of the species of Heteropteryginae is presented and a list summarising all taxonomic changes presented herein.
Here, taxonomic notes on species from three genera of bark crickets are presented. A new locality is recorded for Duolandrevus (Bejorama) parvulus Gorochov, 2016: Singapore. Two new species of Landrevinae are described: one species of Endodrelanva Gorochov, 1999 from Singapore: Endodrelanva jimini sp. nov.; one species of Odontogryllodes Chopard, 1969 from Fraser's Hill, Peninsular Malaysia: Odontogryllodes gratus sp. nov. The male of Odontogryllodes latus Chopard, 1969 is also described for the first time and female is redescribed. Keys to all known species of Endodrelanva and Odontogryllodes is provided.
A new species of the insect order Zoraptera, Zorotypus weiweii, is described and figured from Sabah, East Malaysia. The new species represents the second angel insect from Borneo. Z. caudelli Karny was also collected near the type locality of Z. weiweii. Methods of specimen collection and a brief note of angel insects in Malaysia were provided based on new materials and biological observations.
An integrative taxonomic analysis is used to delimit and describe three new species of Pseudocalotoes from the sky island archipelago of the Banjaran (=mountain range) Titiwangsa of Peninsular Malaysia. Pseudocalotes drogon sp. nov., from Fraser's Hill, Pahang is basal to the sister species P. larutensis from Bukit Larut, Perak in the Banjaran Bintang and the new species P. rhaegal sp. nov. from Cameron Highlands, Pahang. Pseudocalotes drogon sp. nov. is differentiated from all other species of Psuedocalotes by having the combination of a flat rostrum; seven postrostrals; an interparietal; 11 circumorbitals; five canthals; 7-10 superciliaries; one scale between the rostral and nasal; nine supralabials; eight infralabials; 10 postnasal-suborbital scales; four postmentals; five or six sublabials; five or six chinshields; 47 smooth, wide, gular scales; weak transverse gular and antehumeral folds; two enlarged scales between the ear and eye; enlarged upper and lower posttemporals; a single enlarged supratympanic; no enlarged postrictals; three large scales bordering the dorsal margin of the ear opening; large pretympanic scales; eight scales in the nuchal crest not separated by a gap; enlarged vertebral scales extending to the tip of the tail; keeled and non-plate-like scales on flanks; 51 midbody scales; midventrals smaller than dorsals; 19 subdigital lamellae on the fourth finger; 23 subdigital lamellae on the fourth toe; preaxial scales on third toe enlarged and spinose; subdigital lamellae not unicarinate; HW/HL 0.52; HL/SVL 0.31; no elbow or knee patches; and a male dewlap color of lime-green bearing a central yellow spot. Pseudocalotes rhaegal sp. nov. is differentiated from all other Psuedocalotes by having the combination of a convex rostrum; 6-8 postrostrals; an interparietal; nine or 10 circumorbitals; five canthals; 7-10 superciliaries; one or two scales between the rostral and nasal scales; eight or nine supralabials; seven or eight infralabials; 11 or 12 postnasal-suborbital scales; four postmentals; four or five chinshields; 40-45 smooth, wide, gular scales; no transverse gular fold; a weak antehumeral fold; three or four enlarged scales between the ear and eye; an enlarged upper and lower posttemporal; an enlarged supratympanic; no enlarged postrictals; no large scales bordering the upper margin of the ear opening or in the pretympanic region; 6-8 enlarged nuchal crest scales not separated by a gap; enlarged vertebral scales extending to the base of the tail; weakly keeled, non-plate-like scales on the flanks; 52-58 midbody scales; midventrals smaller than dorsals; 19-21 subdigital lamellae on the fourth finger; 22-26 subdigital lamellae on the fourth toe; preaxial scales on the third enlarged and rounded; subdigital lamellae not unicarinate; HW/HL 0.50-0.54; HL/SVL 0.28-0.30; no elbow or knee patches; and female dewlap color yellow bearing a purple base. The analyses also indicated that the new species, P. viserion sp. nov. from Genting Highlands, Pahang in the southern section of the Banjaran Titiwangsa is the sister species of P. flavigula from Cameron Highlands 121 km to the north and can be separated from all other species of Psuedocalotes by having the combination of three postrostrals; 10 circumorbitals; four or five canthals; 5-7 superciliaries; rostral and nasals in contact; supralabials contacting the nasal; six or seven supralabials; six or seven infralabials; two or three postmentals; 47 or 48 smooth, flat, gular scales; three chinshields; weak transverse gular and antehumeral folds; two enlarged scales between the ear and eye; an enlarged upper and lower posttemporal; an enlarged supratympanic; no enlarged postrictals; 7-9 nuchal crest scales lacking gaps and not extending beyond midbody; weakly keeled and plate-like scales on the flanks; 35-38 midbody scales; ventrals smaller than dorsals; 22 or 23 subdigital lamellae on the fourth finger; 26 or 27 subdigital lamellae on the fourth toe; preaxial scales on the third toe not modified; subdigital scales not unicarinate; HW/HL 0.62; no white marking below the eye; dewlap in males yellow; and no elbow or knee patches. Pseudocalotes rhaegal sp. nov. most likely occurs in syntopy with P. flavigula in Tanah Rata at Cameron Highlands and its discovery adds to a growing body of literature detailing the recent descriptions of several new, upland, closely related, sympatric species in Peninsular Malaysia. Another new population referred to here as Pseudocalotes sp. nov. from the Hala-Bala Wildlife Sanctuary, Betong District, Yala Province, Thailand is discussed. The discovery and description of these three new Pseudocalotes from the upland regions of Peninsular Malaysia continues to underscore the remarkably high herpetological diversity and ecological complexity in this sky island archipelago that is still underestimated, unappreciated, and unprotected.
A new species of Bent-toed Gecko, Cyrtodactylus gunungsenyumensis sp. nov. of the sworderi complex, is described from Hutan Lipur Gunung Senyum, Pahang, Peninsular Malaysia and is differentiated from all other species in the sworderi complex by having a unique combination of characters including a maximum SVL of 74.7 mm; low, rounded, weakly keeled, body tubercles; 34-40 paravertebral tubercles; weak ventrolateral body fold lacking tubercles; 38-41 ventral scales; an abrupt transition between the posterior and ventral femoral scales; 20-23 subdigital lamellae on the fourth toe; enlarged femoral scales; no femoral or precloacal pores; no precloacal groove; wide caudal bands; and an evenly banded dorsal pattern. Cyrtodactylus gunungsenyumensis sp. nov. is a scansorial, karst forest-adapted specialist endemic to the karst ecosystem surrounding Gunung Senyum and occurs on the vertical walls of the limestone towers as well as the branches, trunks, and leaves of the vegetation in the associated karst forest. Cyrtodactylus gunungsenyumensis sp. nov. is the seventh species of karst forest-adapted Cyrtodactylus and the sixteenth endemic species of karst ecosystem reptile discovered in Peninsular Malaysia in the last seven years from only 12 different karst forests. This is a clear indication that many species remain to be discovered in the approximately 558 isolated karst ecosystems in Peninsular Malaysia not yet surveyed. These data continue to underscore the importance of karst ecosystems as reservoirs of biodiversity and microendemism and that they constitute an important component of Peninsular Malaysia's natural heritage and should be protected from the quarrying interests of foreign industrial companies.
Genus Nishada Moore (1878) was proposed as a monotypic genus, under subfamily Lithosiinae, family Lithosiidae (now Lithosiini), including only Nishada flabrifera Moore (1878) from Calcutta (now as Kolkata), India. The genus is distributed from China to India, Thailand, Malaysia and up to Australia. The Indian fauna of Nishada is reported from North-East Himalayas, West Bengal (Kolkata) and South India. Members of this genus are unmarked, yellow to brown with short and broad wings. Genus Nishada has been taxonomically dealt by many authors but awaits thorough revision.
HISTORY: Hampson (1900) included a total of ten species: Nishada niveola Hampson, 1900, Nishada syntomioides (Walker, 1862), Nishada impervia (Walker, 1865), Nishada marginalis (Felder 1875), Nishada tula Swinhoe, 1900, Nishada nodicornis (Walker 1862), Nishada rotundipennis (Walker 1862), Nishada flabrifera Moore, 1878, Nishada sambara (Moore 1859) and Nishada xantholoma (Snellen 1879). Swinhoe (1902) and Hampson (1911) then described two new species, Nishada melanistis and Nishada brunneipennis, respectively, followed by Rothschild (1912, 1913) who described a further seven new species, Nishada brunnea, Nishada flavens, Nishada testacea, Nishada griseoflava, Nishada fuscofascia, Nishada louisiadensis and Nishada aurantiaca, bringing the total to 19 species. Strand (1922) catalogued only 13 of these species in Nishada, transferring N. brunnea and N. fuscofascia to genus Scoliacma Meyrick (1886); N. testacea, N.griseoflava and N. louisiadensis Rothschild to Eilema Hübner (1819) and synonymising N. flavens with N. sambara. Next, Matsumura (1927) described N. formosibia, followed by two more species, N. aureocincta Debauche, 1938 and N. benjaminea Roepke, 1946. Holloway (2001) synonymised N. nodicornis with N. rotundipennis and added the description of a new subspecies, Nishada chilomorpha adunca Holloway, 2001 from Borneo, indicating a distributional range as far as North East India. The nominotypical subspecies, N. c. chilomorpha was suggested to be restricted to its type locality of Java. Bucsek (2012) added Nishada cameronensis, Dubatolov & Bucsek (2013) described Nishada schintlmeisteri and Bucsek (2016) described Nishada temenggora. So, at present, Nishada comprises19 species, of which three are known from India (Singh et al. 2014). Herein, we describe one further species, Nishada pseudochilomorpha Joshi & Singh sp. nov., from Jatinga (Assam, India). In addition, new distributional records are reported for N. flabrifera.
The genus Morphosphaera Baly, 1861 is revised. Eleven species are considered as valid, including, M. takizawai sp. nov. (Mt. Basor, 90 km N of Gua Musang, Malaysia, W. Kelantan), described from Malaysia and Indonesia. Color photos of habitus and drawings of diagnostic characters from eleven species are presented. The following synonymies are proposed: M. sodalis Chen, 1935 and M. brunnea Maulik, 1936 are junior synonyms of M. albipennis Allard, 1889; M. margaritacea Laboissière, 1930, M. viridipennis Laboissière, 1930, and M. prava Maulik, 1936 are junior synonyms of M. coomani Laboissière, 1930; M. gracilicornis Chen, 1963 is a junior synonym of M. maculicollis Baly, 1861; M. cavaleriei Laboissière, 1930, M. cincticollis Laboissière, 1930, M. marginata Laboissière, 1930, M. purpurea Laboissière, 1930, M. gingkoae Gressitt & Kimoto, 1963, and M. metallescens Gressitt & Kimoto, 1963 are junior synonyms of M. sumatrana Jacoby, 1886. The type material of M. impunctata Allard, 1890 from the Philippines was not found and its taxonomic status remains uncertain. Morphosphaera peregrina Weise, 1913 is transferred to the genus Borneola Mohamedsaid, 1998 nov. comb. A neotype is designated for Chrysomela japonica Hornstedt, 1788. Lectotypes are designated for the following species: Adorium chrysomeloides Bates, 1866, A. japonicum Baly, 1874, Morphosphaera albipennis Allard, 1889, M. bimaculata Chûjô, 1938, M. caerulea Jacoby, 1896, M. cavaleriei Laboissière, 1930, M. collaris Laboissière, 1930, M. formosa Laboissière, 1930, M. marginata Laboissière, 1930, M. montivaga Maulik, 1936, M. prava Maulik, 1936, M. purpurea Laboissière, 1930, M. sumatrana Jacoby, 1886, M. viridipennis Laboissière, 1930, and Galerucida simplex Weise, 1922.
A new species Leptogomphus tioman is described based on male specimens collected from Tioman Island, Peninsular Malaysia. It is close to Leptogomphus risi Laidlaw in thoracic markings but is readily distinguished by its anal appendages and accessory genitalia.
The ground beetle genus Hexachaetus Chaudoir, 1871 is re-defined and reviewed. Bearing six setae on ligula is no more considered as a crucial characteristic for Hexachaetus. Members of Hexachaetus share the following combination of morphological features: body polish, smooth, and impunctate, ligula more or less dilated at apex, bearing 4, 6, or even 12 setae apically, prosternal process unbordered at apex, elytra distinctly and obliquely truncated at apex, with the apical inner angles very sharp in most species (except for H. mulan n. sp.), and interval 3 with anterior and posterior setiferous pores (median one lacking). The members of Hexachaetus are about 20 species which could be divided into six species groups. All except angulatus species group are dealt with in this paper, with descriptions of four new species: H. kirschenhoferi n. sp. (Indonesia: Kalimantan), H. brunki n. sp. (Malaysia: N. Borneo), H. vietnamensis n. sp. (Vietnam: Annam) and H. mulan n. sp. (Malaysia: Perak and Pahang). H. maindroni Tian & Deuve, 2006 is proposed as a subspecies of H. lateralis Guérin, 1843, n. stat. A key to species groups and species of the genus is also provided.
Coeliccia matok sp. nov. (holotype male from Borneo, Sarawak, Samarahan Division, peat swamp forest at old UNIMAS campus, 25 ii 2008, to be deposited in BMNH) and Coeliccia paludensis sp. nov. (holotype male from Borneo, Kalimantan Tengah, peat swamp forest in ex Mega Rice Project Block E, 18 vi 2012, in RMNH) are described from Borneo. The two new species are apparently confined to peat swamp forest (C. paludensis) or largely confined to peat swamp forest and related forest formations (C. matok). Coeliccia macrostigma Laidlaw is redescribed and all available information on it is summarised. Additional terminology for characters of the prothorax in Coeliccia species is introduced. Distribution maps are given for all three species considered.
The final instar larva of Acrogomphus jubilaris Lieftinck, 1964, is described and figured for the first time based on exuviae from four male and one female larvae collected in Sarawak, Malaysian Borneo. The adults of A. jubilaris are very rarely encountered. The larvae, however, are surprisingly common in forest streams in Borneo. It is compared with A. malayanus Laidlaw, 1925 and A. walshae Lieftinck, 1935, and notes on behavior, distribution and habitat are included. A map including all known records of A. jubilaris is provided.
Two new medium-sized whiprays, Maculabatis arabica sp. nov. and M. bineeshi sp. nov., are described from specimens collected in coastal habitats of the northern Indian Ocean, off India and Pakistan. Both species superficially resemble M. randalli (Last, Manjaji-Matsumoto & Moore), and appear to have been confused with a more widely distributed whipray M. gerrardi Gray, and another undescribed species from the Indian Ocean. Maculabatis arabica sp. nov. (attains at least 63 cm DW) is diagnosed by a combination of external characters, i.e. morphometrics (e.g. relatively short disc, narrow interspaces between paired structures on the head), squamation (relatively slow denticle development and a characteristic denticle band shape), plain dorsal disc coloration (rather than spotted), and tail light brown and banded beyond the caudal sting in juveniles but almost plain in adults. Maculabatis bineeshi sp. nov. (attains at least 66 cm DW) is diagnosed by a combination of characters, i.e. morphometrics (e.g. suboval to weakly rhombic disc in young), squamation (rapid denticle development and broad denticle band with margins truncate near pectoral-fin insertions), plain dorsal disc coloration (no white spots), and a dark blackish tail (especially in young) with weakly mottled banding on its dorsal surface beyond the caudal sting. Maculabatis arabica sp. nov. appears to be confined to the Arabian Sea (from Pakistan to western India), whereas M. bineeshi sp. nov. occurs in the Arabian Sea (off Pakistan and northwestern India) and in the Bay of Bengal (confirmed off Odisha, eastern India).
New additions to the knowledge of the subfamily Eumeninae are provided. Eight new species of Eumeninae are described: Antepipona gibbosissima Selis, sp. nov. (Namibia: Warmbad); Antepipona tricolorata Selis, sp. nov. (India: Sikkim); Ectopioglossa luzonica Selis, sp. nov. (Philippines: Luzon); Lissodynerus unicus Selis, sp. nov. (India: Sikkim); Pararrhynchium aurigaster Selis, sp. nov. (Malaysia: Johor); Symmorphus (Symmorphus) incisus Selis, sp. nov. (India: Sikkim); Symmorphus (Symmorphus) palawanensis Selis, sp. nov. (Philippines: Palawan); Zethus (Zethus) intermedius Selis, sp. nov. (Burkina Faso). The male of Synagris (Paragris) biplagiata Gusenleitner, 2005 is described. New distributional data for other species are provided.
A new species of the portunid genus, Monomia Gistel, 1848, is described from the South China Sea in Vietnam. Monomia lucida sp. nov. is morphologically most similar to M. argentata (A. Milne-Edwards, 1861), which was originally described from Sarawak, on the island of Borneo. In addition to the stout, forward-directed anterolateral teeth of the carapace, the subrectangular sixth segment of the male pleon, and the long and slender laterally bent first gonopods, adults of the new species reach a greater size, and can also be distinguished from M. argentata by the colour pattern on the natatory dactylus. The independent specific status of M. lucida sp. nov. is also supported by molecular evidence. Aside from a comparison of this new species with other known congeners, new photographs of the holotype of M. samoensis (Ward, 1939) are also provided.
Rhabdamia spilota Allen Kuiter 1994 (Apogonidae), a poorly known cardinalfish previously known only from the Philippines, Indonesia and the Red Sea, is redescribed on the basis of 70 specimens (20.9-61.2 mm standard length) (including types), from the Indo-West Pacific (Red Sea, Andaman Sea, Japan, South China Sea, the Philippines, Indonesia, New Caledonia, and Australia). Because most reports of the similar species R. gracilis (Bleeker 1856), following its original description, were based on misidentifications, R. gracilis is also redescribed (based on 98 Indo-West Pacific specimens from Seychelles, Maldives, Andaman Sea, Japan, Malaysia, Indonesia, New Caledonia, and Australia, 27.9-59.3 mm standard length); a lectotype is designated for it. Rhabdamia spilota differs from R. gracilis in having 27-33 (mode 30-31) developed gill rakers [vs. 22-27 (mode 24) in the latter], 27-33 (30) gill rakers including rudiments [vs. 23-27 (24-25)], a black stripe from the jaw tips to the anterior margin of the orbit (vs. black pigments only at snout and tip of lower jaw), 3-6 reddish brown to blackish blotches on the opercle and anterior of body (vs. blotches absent), and indistinct black pigment restricted to caudal fin outer margins (vs. pigment scattered over entire fin). Rhabdamia gracilis exhibits sexual dichromatism, female specimens larger than 41.3 mm SL having one or two black stripes on the lateral surface of the body; the stripes are absent in males and smaller females. No evidence of sexual dichromatism was found in R. spilota.
Platybaetis bishopi Müller-Liebenau, 1980 was originally described from Malaysia only at the larval stage. We provide the first description of the imaginal stage of P. bishopi based on materials from Thailand. The imago of this species can be separated from the known species by coloration of abdominal terga and coloration of wings. A new species, Platybaetis nayokensis sp. nov., is described based on male and female imagos and larvae from Thailand. The larva of this species is mainly distinguished by medium acute spines on the posterior margin of the abdominal terga and two apical setae on the glossa, which seem to be shorter than in other species. The imago can be separated by the abdominal color pattern. The larva of this genus is adapted to live on wet rocks projecting out of water; it prefers large stones near small waterfalls or areas between two large rocks in running water.
Drepanosticta emtrai sp. nov. is described from Vietnam (holotype male Ha Tinh Province, 9 vi 2015, to be deposited in RMNH). The new species is allied to D. carmichaeli (Laidlaw, 1915) and a number of other species of Drepanosticta including D. vietnamica Asahina, 1997. New illustrations of the paratype of D. vietnamica are provided and the species is discussed. The Drepanosticta carmichaeli-group, to which the above mentioned species belong, is defined and discussed.
Drepanosticta adenani sp. nov. (holotype ♂, from a tributary of Sungai Jela, Nanga Segerak area, Lanjak Entimau Wildlife Sanctuary, Sri Aman Division, Sarawak, Malaysian Borneo, 18 vii 2016, deposited in the Natural History Museum, London) is described from both sexes.